Transition from absolute to quantitative short-day control in Nicotiana tabacum cv. Maryland Mammoth

The response in vitro of thin cell layers, excised from different stem regions of Nicotiana tabacum cv. Maryland Mammoth plants at various developmental stages, was studied under different photoperiodic treatments. The aim was to determine at which stage of plant development, and in which region of the stem, the absolute short-day requirement, indispensable for the induction of the flowering process in this genotype, becomes quantitative and whether it remains short-day. The explants were cultured on a medium suitable for flower neoformation, and were exposed for 30 days to the following treatments: continuous darkness, 8 h light/16 h dark per day, 16 h light/8 h dark per day, and continuous light. The first flowers on explants were observed from plants that were still in the vegetative state, but whose apex showed an accelerated production of axillary vegetative buds, as observed histologically. These explants were excised from the first 10 internodes below the first node with a leaf ≥ 5 cm in length (apical site), and produced flowers only under short-day treatment. When the apical dome initiated the organization of the terminal flower, the apical site explants developed flowers under both short-day and long-day treatments. At the same stage, explants from the 15th to the 20th internode below the first leaf ≥ 5 cm in length also formed flowers, but only under short-day. When the plant showed a complete inflorescence, flowers were also present on explants from the most basal stem internodes and from the inflorescence branches. At this stage, flower neoformation occurred under all treatments; however, under short-day the number of explants showing flowers not associated with vegetative buds on the same sample greatly exceeded that observed under other treatments, as did the mean number of flowers per explant (except the basal regions). In conclusion, in the post-inductive phases of the flowering process, the photoperiodic requirement of this genotype is always short-day. The superficial tissues of the stem require either absolute or quantitative short-day treatment, depending on their position on the stem and the stage of evolution of the flowering process in the terminal apex.     

Effect of Photoperiod and Chlorogenic Acid on Morphogenesis in Leaf Discs of Streptocarpus Nobilis

Leaf discs from vegetative plants greatly increase their phenolic content when cultivated in vitro. Under long days the values remained constant, and were higher when compared with short days cultures. Under short days total phenolics decreased after 10 d, corresponding to the induction and expression of in vitro flowering. The effect of photoperiod and chlorogenic acid (0.01 mM) on leaf discs cultured from induced and non-induced plants, were analyzed regarding the neo-formation of roots, as well as vegetative and flower buds. Chlorogenic acid enhances the regeneration of roots in all treatments tested, with the highest stimulation on induced leaf discs cultivated in short days. The flowering was not affected by chlorogenic acid, but an inhibitory effect was observed on the neo-formation of vegetative buds in non-induced explants maintained in short days. Vegetative buds were reduced by 50% in flower-induced leaf discs cultivated under short days.     

Further experiments on spermidine-mediated floral-bud formation in thin-layer explants of Wisconsin 38 tobacco

We studied the effects of various polyamines on bud regeneration in thin-layer tissue explants of vegetative and floweringNicotiana tabacum L. cv. Wisconsin 38, in which application of exogenous spermidine (Spd) to vegetative cultures causes the initiation and development of some flower buds (Kaur-Sawhney et al. 1988 Planta173, 282). We now show that this effect is dependent on the time and duration of application, Spd being required from the start of the cultures for about three weeks. Neither putrescine nor spermine is effective in the concentration range tested. Spermidine cannot replace kinetin (N⁶-furfurylaminopurine) in cultures at the time of floral bud formation, but once the buds are initiated in the presence of kinetin, addition of Spd to the medium greatly increases the number of floral buds that develop into normal flowers. Addition of Spd to similar cultures derived from young, non-flowering plants did not cause the appearance of floral buds but rather induced a profusion of vegetative buds. These results indicate a morphogenetic role of Spd in bud differentiation. Dedicated to Professor Hans Mohr on the occasion of his 60th birthday     

In-vitro flower formation in leaf explants of tomato: effect of NaCl

Leaf explants of 24 cultivars and 2 F1 hybrids of the common tomato (Lycopersicon esculentum Mill.) and ofL. pimpinellifolium Brezh. were cultured on Murashige-Skoog medium containing different concentrations of NaCl. The cultures of 11 genotypes formed flower buds when cultured on medium containing 0.5% NaCl. Flower formation occurred either by direct differentiation from the leaf cultures or by transition of the apices of regenerated shoots from the vegetative state to floral buds. No flower formation occurred on medium without NaCl or media with 1.0% NaCl or more. There existed great differences in the capacity of in-vitro flower formation in the tomato leaf explants among the genotypes tested. The genotypes whose explants did form flowers were all of determinate growth habit.     

Flower formation in vitro in a quantitative short-day tobacco: interrelation between photoperiod and infructescence development

The flowering response of thin layers excised from branch internodes of Nicotiana tabacum cv. Maryland Catterton (quantitative short-day plant for induction) was studied under three photoperiodic treatments. The explants were excised from inflorescences bearing flowers only, flowers and green fruits, or from infructescences with green fruits only. The aim of the study was to investigate the post-inductive photoperiodic effects on in vitro flower bud formation in a quantitative short-day tobacco and the relation with infructescence development. Short days quantitatively enhanced the flower bud regeneration capacities of explants in all stages of development, both as number of explants induced to produce flowers and as mean number of flowers per explant. There was no significant difference in flower bud formation on explants of the first two stages, which produced much more flowers than those of the third stage. Observations in planta showed that, during the 20 days separating the second stage from the first stage, there was no significant difference in the number of floral buds and flowers present on the inflorescence; however, the branch internodes lengthened, as did the floral buds and flowers. During the 10 days leading to the third stage, the number of capsules did not change significantly, but a high rate of floral abscission occurred. The present results show that in Nicotiana tabacum cv. Maryland Catterton short day quantitatively controls not only the inductive step of the flowering process, but also affects the capacity to regenerate flower buds during the late post-inductive phases. The responsiveness to the photoperiodic signal decreases only when the plant exhibits only fruits.     

Exogenous Ca2+ alleviates waterlogging-caused damages to pepper

Ca²⁺ has been considered as a necessary ion for alleviation of stress-induced damages in plants. We investigated effects of exogenous Ca²⁺ on waterlogging-induced damage to pepper and its underlying mechanisms. Pepper seedlings under stress were treated by spraying of 10 mM CaCl₂. Applying exogenous Ca²⁺ increased the biomass of pepper leaves and roots, improved photosynthetic characteristics, membrane permeability, root activity, osmotic substance contents, antioxidant enzyme and alcohol dehydrogenase activities, while it reduced lactate dehydrogenase activity. It maintained hydroxide radical contents and activities of malate dehydrogenase and succinate dehydrogenase relatively high. Our results suggested that applying exogenous Ca²⁺ could regulate osmotic substance contents, antioxidant system activity, root respiration, and metabolism, and subsequently alleviate waterlogging-induced damages to pepper plants.     

Tissue distribution and biosynthesis of 1,2-saturated pyrrolizidine alkaloids in Phalaenopsis hybrids (Orchidaceae)

Phalaenopsis hybrids contain two 1,2-saturated pyrrolizidine monoesters, T-phalaenopsine (necine base trachelanthamidine) and its stereoisomer Is-phalaenopsine (necine base isoretronecanol). T-Phalaenopsine is the major alkaloid accounting for more than 90% of total alkaloid. About equal amounts of alkaloid were genuinely present as free base and its N-oxide. The structures were confirmed by GC-MS. The quantitative distribution of phalaenopsine in various organs and tissues of vegetative rosette plants and flowering plants revealed alkaloid in all tissues. The highest concentrations were found in young and developing tissues (e.g., root tips and young leaves), peripheral tissues (e.g., of flower stalks) and reproductive organs (flower buds and flowers). Within flowers, parts that usually attract insect visitors (e.g., labellum with colorful crests as well as column and pollinia) show the highest alkaloid levels. Tracer feeding experiments with (14)C-labeled putrecine revealed that in rosette plants the aerial roots were the sites of phalaenopsine biosynthesis. However active biosynthesis was only observed in roots still attached to the plant but not in excised roots. There is a slow but substantial translocation of newly synthesized alkaloid from the roots to other plant organs. A long-term tracer experiment revealed that phalaenopsine shows neither turnover nor degradation. The results are discussed in the context of a polyphyletic molecular origin of the biosynthetic pathways of pyrrolizidine alkaloids in various scattered angiosperm taxa. The ecological role of the so called non-toxic 1,2-saturated pyrrolizidine alkaloids is discussed in comparison to the pro-toxic 1,2-unsaturated pyrrolizidine alkaloids. Evidence from the plant-insect interphase is presented indicating a substantial role of the 1,2-saturated alkaloids in plant and insect defense.     

The induction of flowering in vitro in stem segments of Plumbago indica L.

Summary Internode segments excised from vegetative Plumbago indica plants are responsive to photoperiodic treatments in vitro. Under long days, they produce vegetative buds; under short days, they develop inflorescences. These inflorescences can remain devoid of flowers (vegetative inflorescences), or produce normal flowers which open in the test tubes. The minimum duration of the short-day treatment capable of inducing flowering is of the order of 4 weeks.The production of inflorescences under short days is affected by various factors. An adequate level of sucrose is necessary. Sucrose can be replaced by maltose and, to a small extent, by cellobiose, but not by mannitol or lactose. Auxins and gibberellins inhibit the production of flower buds, whereas cytokinins and adenine do not. Guanine, thymine, cytosine or uracil alone are ineffective, but thymine or its precursor, orotic acid, enhance the production of floral buds when adenine and kinetin are also present in the medium. Several amino acids, as well as glutamine and asparagine, tend to reduce inflorescence formation at 3×10^-4 M or above; urea increases it slightly at the same concentrations. Both the cis- and the trans-isomer of abscisin II enhance inflorescence formation under short days, but have no such effect under long days.High concentrations of adenine re-established the red coloration of the petals which is typical of the clone used. Otherwise, the color of the flowers grown in vitro was pink, presumably because of the depressing effect of kinetin on anthocyanin synthesis.The techniques used have been described in the preceding article (Nitsch and Nitsch, 1966). All segments were excised from internodes of stock plants kept in completely vegetative conditions in a greenhouse by means of 16-hour photoperiods.     

The protein of rolB gene enhances shoot formation in tobacco leaf explants and thin cell layers from plants in different physiological states

The objective was to determine whether the protein of rolB affects shoot formation and whether this potential relationship depends on the developmental stages of the plant and/or on the culture conditions. Thin cell layers (TCL) and leaf explants were excised from tobacco plants in the vegetative and flowering stages and cultured under various hormonal conditions. In TCLs of vegetative-stage plants, the expression of rolB enhanced the formation of the shoot buds under hormone-free conditions and with specific concentrations of auxin and/or cytokinin. Histological examination showed that the induction of the shoot meristemoids was particularly enhanced by rolB protein and that meristemoid growth was accelerated. In leaf explants from vegetative-stage plants, the expression of rolB increased the formation of shoot buds in the presence of 1 M IAA plus 1 or 10 M cytokinin. With BA alone, at a 0.1 M concentration, shoot formation occurred in the transgenic explants only, whereas with concentrations ranging from 0.5 to 10 M, it was higher in these explants than in controls.RolB protein enhanced the formation of shoot buds in TCLs from flowering plants under all hormonal conditions. In the presence of 1 M IAA and kinetin, the protein also increased the flowering response. In leaf explants from flowering plants, the expression of rolB increased the number of shoot buds in the presence of 1 M IAA with 10 M BA.In conclusion, rolB protein promotes shoot formation; it seems to have a positive interaction with cytokinin and an effect on the induction of the meristematic condition.     

Effects of some growth regulators on in vitro flowering of Streptocarpus nobilis

Leaf discs from vegetative Streptocarpus nobilis plants were cultured in vitro in media with cytokinin (BAP or K at 0.35 mg.1^?1) and auxin (IAA, NAA or 2,4-D at 0.1 mg.1^?1). Under short days (8-h photoperiod) in medium with IAA and BAP, floral buds developed in 100% of the cultures; under long days (16-h photoperiod) only shoots were formed. In medium with IAA and K, flowering was reduced. Flowers rarely formed in medium containing NAA and K, but roots developed profusely. NAA + BAP promoted leafy shoots which rarely flowered later. The effect of 2,4-D was to inhibit flowering completely and to induce callusing and formation of teratomous structures.     

Floral activity in solutions of deoxyribonucleic Acid extracted from tobacco stems

For Nicotiana tabacum cv. Wis. 38 plants, the capabilities of solutions containing DNA, extracted from either homogenates of stems in a floral state or nuclei of stems in a vegetative state, to effect flowering of vegetative plants have been studied. Previous work indicates that the DNA from homogenates of stems in a floral state is mainly nuclear. If DNA solutions are supplied to axillary buds of vegetative plants and if the axillary buds are defoliated every 4th day for 12 days, the buds supplied a solution of DNA from stems in a floral state initiate flowers under noninductive conditions, and the buds supplied a solution of DNA from stems in a vegetative state remain vegetative. Heating and rapidly cooling a solution of DNA from stems in a floral state enhances its floral activity. Heating and cooling a DNA solution also results in novel flowers showing up in many treated plants. Novel flowers are more striking in the offspring than in the parents. The capabilities of heated-cooled DNA solution to initiate flowers in noninductive conditions and to cause novel flowers are eliminated completely by treating (before heating and cooling) the DNA solution with deoxyribonuclease. Heated-cooled solutions of DNA extracted from nuclei of either vegetative stems or vegetative leaves contain no floral activity.     

Protease activity, organisation of vegetative primordia and effect of putrescine in tobacco thin layers

Since in tobacco thin layers exogenous putrescine alters the physiological and mor-phogenic responses induced by IAA (indole-3-acetic acid) and/or BA (benzylade-nine), the effect of this polyamine on protease activity and on the formation of meristemoids and vegetative primordia was studied during morphogenesis. Superficial thin layer explants, excised from the stem of tobacco (Nicotiana tabacum L. cv. Samsun) plants in the vegetative stage, were cultured under various hormonal conditions (IAA, IAA+BA, BA) and in a hormone-free medium, in the presence or absence of 100 μM putrescine. Histological analysis showed that no meristemoids were formed on the control medium or with putrescine alone and only a few were formed on IAA-treated explants with or without putrescine. An increasing number of meristemoids was observed in IAA+BA and BA treatments during culture; in both cases this number was enhanced by the presence of exogenous putrescine. Protease activity was evaluated spectrophotometrically using two synthetic substrates, azocasein and N-benzoyl-DL-arginine-p-nitroanilide (BAPNA). In the former, maximum protease activity was observed in IAA+BA- and BA-treated explants on days 10 and 15, respectively, while with IAA activity was lowest, the maximum occurring on days 5–10. In this case exogenous putrescine enhanced protease activity in the presence of IAA alone or with BA, while it decreased it in the presence of BA. BAPNA-mediated proteolytic activity (serine-proteases) was highest in IAA+BA-treated explants, intermediate in BA- and not different from controls in IAA-treated explants. Putrescine only affected proteolytic activity in IAA+BA treatments. The use of specific inhibitors of protease activities indicated that these enzymes belong to two main classes of proteases, that is serine- and thiol-proteases. The pattern of proteolytic activities during culture appeared to be related to the differentiation of meristemoids into vegetative primordia. The effect of exogenous putrescine on protease activity was different depending on different synthetic substrates, developmental patterns, pH and ionic strength.     

Capacité caulogène de cellules de cal issues des couches cellulaires minces de type épidermique de ramifications florales de Nicotiana tabacum cv. Wise. 38 Par

Bud formation capacity of callus formed from thin epidermal cell loyers excised from floral branches of Nicotiana tabacum cv. Wise. 38. Subepidermal cells of thin tissue pieces with a few cell layers were capable of forming eitber buds, roots, (lowers or non-organ ogenetic callus. To determine wheiher this calltjs is able to dirferentiate into organs, we transferred it to media inducing eitber flowers, or buds, or roots. In this paper, we study ibe capacity of lbe callus to form buds. In 50% of the cases, the explants (being maintained for I day to 2 years in callus media) can still express the capacity to form buds. This percentage increased with increased agar concentration of the culture media. At the histological level, non-organogenetic callus is characterized by the absence of tracheid differentiation, whereas in the organogenetic callus, iracheids were induced after their transfer into a ‘Bud medium’ and indicate an organogenetic differentiation pattern.     

The effect of carbon source on callus induction and regeneration ability in Pharbitis nil

Flower buds, cotyledons and hypocotyls of Pharbitis nil were used as plant material. Flower buds (1–2 mm long) were excised from 3-week-old plants, grown in soil. Cotyledons of 7-day-old sterile seedlings were cut into 25 mm² squares cotyledons whereas hypocotyls were cut to 1 mm long fragments. Explants were transferred into Petri dishes containing the Murashige and Skoog medium (MS), supplemented with either BA (11 μM·L⁻¹) alone or BA (22 μM·L⁻¹) and NAA (0.55 μM·L⁻¹), and different sugars: sucrose, fructose, glucose, mannose or sorbitol (autoclaved or filter-sterilized). Addition of glucose instead of sucrose to the medium stimulated the induction of callus on flower buds and cotyledonary explants, but inhibited its growth on fragments of hypocotyls. The medium supplemented with fructose (especially filter-sterilized) stimulated the development of flower elements. Organogenesis of shoots and roots on explants was also observed. Flower buds and hypocotyls were able to regenerate both organs. Addition of fructose or glucose to the medium stimulated the organogenesis of shoots, whereas root organogenesis was inhibited on all explants used. Sorbitol strongly inhibited both induction of callus and organogenesis on all explants used.     

The effect of photoperiod on flower formation in vitro in a quantitative short-day cultivar of Nicotiana tabacum

Superficial cell layers of a quantitative short-day tobacco plant ( Nicotiana tabacum L. cv. White Burley) were excised from different parts of the inflorescence (i.e. pedicels, branch internodes, rachises), and cultured in continuous darkness, continuous light or 8 h light/16 h dark daily. The flowering response in vitro of the different types of explants was investigated with respect to the effect of light on the post-evocation phases of the flowering process and explant commitment. Treatment effect was qualitatively and quantitatively influenced by explant origin. Three morphogenic features were observed: flower neoformation, caulogenesis and rhizogenesis (the latter on rachis explants only). Under all treatments, the highest flowering potential was shown by pedicels, while the highest vegetative potential was shown by rachises. Branch internodes showed an intermediate response, but with a tendency towards caulogenesis, which probably reflects their phylogenetic origin. Thus, opposite gradients of the neoformation of flowering and vegetative buds on explants were observed under all treatments. Pedicels formed new single flowers rather than inflorescences, while rachises regenerated mainly inflorescences. In darkness, flowering was limited mostly to pedicels. Vegetative bud formation was higher than floral bud regeneration in all types of explant. Continuous light enhanced the flowering response mostly in pedicel and branch internode explants. Short days enhanced flower bud formation in vitro on all types of explant. Results with respect to microsporogenesis, flower and inflorescence anomalies observed under darkness also seem to support the existence of a quantitative photoperiodic control on floral neoformation in vitro in this plant. These results suggest that in Nicotiana tabacum cv. White Burley in vivo floral induction, initiation and development are governed by the same photoperiodic requirements.     

Shoot regeneration of dwarf dogwood (Cornus canadensis L.) and morphological characterization of the regenerated plants

Dwarf dogwoods (or the bunchberries) are the only suffrutex in Cornaceae. They are attractive ground cover ornamentals with clusters of small flowers surrounded by petaloid bracts. Little has been reported on plant regeneration of dogwoods. As a step toward unraveling the molecular basis of inflorescence evolution in Cornus, we report an efficient regeneration system for a dwarf dogwood species C. canadensis through organogenesis from rejuvenated leaves, and characterize the development of the plantlets. We used the nodal stem segments of vegetative branches as explants. Micropropogated shoots were quickly induced from axillary buds of nodes on an induction medium consisting of basal MS medium supplemented with 4.44 μM BAP and 0.54 μM NAA. The new leaves of adventitious shoots were used as explants to induce calli on the same induction medium. Nearly 65% of leaf explants produced calli, 80% of which formed adventitious buds. Gibberellic acid (1.45 μM) added to the same induction medium efficiently promoted quick elongation of most adventitious buds, and 0.49 μM IBA added to the basal MS medium promoted root formation from nearly 50% of the elongated shoots. The growth of plantlets in pot soil was characterized by the development of functional woody rhizomes, which continuously developed new aboveground vegetative branches, but not flowering branches, within the past 12 months. Potential reasons causing the delay of flowering of the regenerated plants are discussed. The establishment of this regeneration system facilitates developing a genetic transformation system to test candidate genes involved in the developmental divergence of inflorescences in Cornus. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

STUDIES ON THE FLORAL HISTOGENESIS AND PHYSIOLOGY OF PERILLA. II. FLORAL INDUCTION IN CULTURED APICAL BUDS OF P. FRUTESCENS

Raghavan , V., and W. P. Jacobs . (Princeton U., Princeton, N. J.) Studies on the floral histogenesis and physiology of Perilla. II. Floral induction in cultured apical buds of P. frutescens. Amer. Jour. Bot. 48(9): 751–760. Illus. 1961.—The morphological and histological changes induced in apical buds and explants of P. frutescens (L.) Britt. var. ‘Tall Late’ in short days and long days when cultured in White's medium have been followed. When photoinduced in culture, apical buds showed visible signs of changes in 30.9 days, and produced normal flowers in 81.6 days. Apical buds in LD showed similar transformations at the apices, but with continued LD treatment, they elongated to form sterile structures, superficially resembling Selaginella cones. The normal flowers formed in culture were similar to those formed on the intact plant, while the individual florets of the LD-cone differentiated only the non-sporogenous tissues in them. A less pronounced sequence of changes resulted when apical buds stripped of their older pairs of apical leaves were LD- or SD-treated. When explants with the 1st pair of unfolded leaves or with the 1st and 2nd pairs of unfolded leaves were photoinduced in vitro, the responses were relatively fast. However, explants with the 1st and 2nd pairs of unfolded leaves in LD remained entirely vegetative. When unfolded leaves were implanted in the same medium separated from the buds and both were photoinduced or given LD, the buds formed the typical 1st signs, but did not differentiate into normal flowers. This inhibition of flowering resulted in the formation of sterile cones, consisting of florets with non-sporogenous tissues only. The results have suggested the possibility of the sterile cone-like structures being an intermediate stage in the flowering of Perilla. The role of a possible inhibitor produced by mature leaves of SD plants in LD is discussed.     

Neo-formation of flower buds and other morphogenetic responses in tissue cultures of Melia azedarach

Melia azedarach has great interest because of its insecticidal properties. Recently, the occurrence of precocious flowering in tissue cultures of this species was reported. This paper describes some in vitro morphogenetic responses using hypocotyl segments as explants and MS basal medium. Amongst the results we report are: (a) in basal medium, 5% of the explants neo-formed floral buds and flowers, and 80% formed vegetative shoots; (b) flower neo-formation could not be controlled or increased by addition of benzyladenine, or lowering the nitrogen level; (c) benzyladenine increased the regeneration of vegetative shoots; (d) compact green calluses were eventually formed in basal medium, and vigorous friable calluses can be easily induced with 0.5 mM 2,4-D; (e) green calluses could be subcultured and regenerated into plants, and, from friable calluses, cell suspensions were started; (f) histological studies showed that neo-formations originate in the wound tissue or from the inner tissue of the hypocotyl.